Lucetam®

Ukraine
Brand name Lucetam®
Form solution for injection
Active substance / Dosage
piracetam · 200 mg/ml
Prescription type prescription only
ATC code
Registration number UA/8165/02/01
Lucetam® solution for injection

Children. Do not use. Overdose. Symptoms: intensification of the drug's adverse effects. Symptoms of overdose were observed with oral administration of the drug at a dose of 75 g. Treatment is symptomatic. There is no specific antidote; hemodialysis can be used (eliminates 50–60% of piracetam). Adverse reactions.

Organ system according to WHO organ classification system

Common
(≥1/100 to <1/10)

Uncommon
(≥1/1000 to <1/100)

Nervous system disorders

Hyperkinesia

Metabolism and nutrition disorders

Weight increased

Psychiatric disorders

Irritability

Depression

General disorders and administration site conditions

Asthenia

Adverse reactions reported during post-marketing surveillance are listed below by system organ classes.

Blood and lymphatic system disorders.
Rare: haemorrhagic disorders.

Immune system disorders.
Rare: hypersensitivity, anaphylactoid reactions.

Psychiatric disorders.
Frequent: nervousness.
Uncommon: depression.
Rare: increased excitability, anxiety, confusion, hallucinations.

Nervous system disorders.
Frequent: hyperkinesia.
Uncommon: somnolence.
Rare: ataxia, loss of balance, increased frequency of epileptic seizures, headache, insomnia, tremor.

Ear and labyrinth disorders.
Rare: dizziness.

Gastrointestinal disorders.
Rare: abdominal pain, upper abdominal pain, diarrhoea, nausea, vomiting.

Skin and subcutaneous tissue disorders.
Rare: angioneurotic oedema, dermatitis, rash, urticaria, pruritus.

Reproductive system and breast disorders.
Rare: increased libido.

Vascular disorders.
Very rare: hypotension, thrombophlebitis.

General disorders and administration site conditions.
Uncommon: asthenia.
Very rare: injection site pain, chills.

Investigations.
Frequent: weight gain.

Shelf life.
3 years.
Do not use the medicinal product after the expiry date stated on the packaging.

Storage conditions.
Store at a temperature not exceeding 25 °C in a place inaccessible to children.

Incompatibilities.
Not applicable. Studies have not been conducted. The medicinal product must not be mixed with other medicinal products.

Packaging.
5 ml (1 g) in an ampoule; 5 ampoules in a blister; 2 blisters in a cardboard box.
15 ml (3 g) in an ampoule; 4 ampoules in a blister; 1 or 5 blisters in a cardboard box.

Prescription status.
Prescription only.

Manufacturer.
EGIS Pharmaceuticals PLC.

Address of the manufacturer and location of operations.
1165 Budapest, Bokenyfoldi ut. 118–120, Hungary.